Polydactyly genes cases retinal dystrophies. Medical search. Frequent questions

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Anatomy20

Toes Fundus Oculi Photoreceptor Cells, Vertebrate Retina Thumb Pigment Epithelium of Eye Photoreceptor Cells Limb Buds Fingers Retinal Pigment Epithelium Extremities Retinal Rod Photoreceptor Cells Retinal Cone Photoreceptor Cells Cilia Hallux Forelimb Chromosomes, Human, Pair 7 Ribs Muscle, Skeletal Rod Cell Outer Segment

Organisms2

Mice, Inbred mdx Rats, Mutant Strains

Diseases60

Polydactyly Retinal Dystrophies Muscular Dystrophies Retinal Degeneration Myotonic Dystrophy Leber Congenital Amaurosis Short Rib-Polydactyly Syndrome Bardet-Biedl Syndrome Muscular Dystrophy, Duchenne Retinitis Pigmentosa Laurence-Moon Syndrome Corneal Dystrophies, Hereditary Muscular Dystrophy, Animal Abnormalities, Multiple Ellis-Van Creveld Syndrome Syndrome Hand Deformities, Congenital Fuchs' Endothelial Dystrophy Retinal Diseases Orofaciodigital Syndromes Syndactyly Eye Diseases, Hereditary Blindness Muscular Dystrophy, Facioscapulohumeral Limb Deformities, Congenital Kidney Diseases, Cystic Microphthalmos Night Blindness Foot Deformities, Congenital Alstrom Syndrome Encephalocele Hand Deformities Muscular Dystrophy, Emery-Dreifuss Usher Syndromes Optic Atrophy, Hereditary, Leber Ectromelia Macular Degeneration Choroid Diseases Neuroaxonal Dystrophies Mouth Abnormalities Optic Atrophies, Hereditary Intellectual Disability Ciliary Motility Disorders Optic Disk Drusen Hypertelorism Hamartoma Congenital Abnormalities Muscular Dystrophy, Oculopharyngeal Thoracic Diseases Reflex Sympathetic Dystrophy Vision Disorders Vitelliform Macular Dystrophy Polycystic Kidney Diseases Dandy-Walker Syndrome Bone Diseases, Developmental Pallister-Hall Syndrome Dwarfism Craniofacial Abnormalities Holoprosencephaly Disease Models, Animal

Chemicals and Drugs23

cis-trans-Isomerases Eye Proteins Peripherins Dystrophin Hedgehog Proteins Group II Chaperonins Cytoplasmic Dyneins Codon, Nonsense Nerve Tissue Proteins Sarcoglycans Proteins Lipofuscin Kruppel-Like Transcription Factors Rhodopsin Membrane Proteins Dystroglycans Utrophin Intermediate Filament Proteins Rod Opsins Carrier Proteins ATP-Binding Cassette Transporters Guanylate Cyclase Fibroblast Growth Factor 4

Analytical, Diagnostic and Therapeutic Techniques and Equipment14

Electroretinography Pedigree DNA Mutational Analysis Visual Acuity Fluorescein Angiography Chromosome Mapping Dermatoglyphics Heteroduplex Analysis Tomography, Optical Coherence Visual Field Tests Ophthalmoscopy Genetic Testing Disease Models, Animal Polymerase Chain Reaction

Psychiatry and Psychology3

Visual Acuity Intellectual Disability Visual Fields

Phenomena and Processes25

Consanguinity Genes, Recessive Mutation Phenotype Genes, Dominant Dark Adaptation Visual Acuity Homozygote Mutation, Missense Genetic Linkage Heterozygote Codon, Nonsense Exons Lod Score Visual Fields Haplotypes Base Sequence Exome Chromosomes, Human, Pair 7 Body Patterning Polymorphism, Single-Stranded Conformational Frameshift Mutation Genotype Amino Acid Sequence Gene Expression Regulation, Developmental

Anthropology, Education, Sociology and Social Phenomena3

Dermatoglyphics Wills Incest

Information Science3

Molecular Sequence Data Base Sequence Amino Acid Sequence

Named Groups1

Infant, Newborn

Health Care2

Age of Onset Genetic Testing

Anatomy Organisms Diseases Chemicals and Drugs Analytical, Diagnostic and Therapeutic Techniques and Equipment Psychiatry and Psychology Phenomena and Processes Anthropology, Education, Sociology and Social Phenomena Information Science Named Groups Health Care

Polydactyly Retinal Dystrophies Muscular Dystrophies Retinal Degeneration Myotonic Dystrophy Leber Congenital Amaurosis Short Rib-Polydactyly Syndrome Bardet-Biedl Syndrome Muscular Dystrophy, Duchenne Retinitis Pigmentosa Toes Laurence-Moon Syndrome Corneal Dystrophies, Hereditary Electroretinography cis-trans-Isomerases Pedigree Consanguinity Muscular Dystrophy, Animal Abnormalities, Multiple Eye Proteins Fundus Oculi Genes, Recessive Ellis-Van Creveld Syndrome Syndrome Hand Deformities, Congenital Fuchs' Endothelial Dystrophy Retinal Diseases Mutation Orofaciodigital Syndromes Syndactyly Eye Diseases, Hereditary Photoreceptor Cells, Vertebrate Retina Peripherins Thumb DNA Mutational Analysis Blindness Phenotype Muscular Dystrophy, Facioscapulohumeral Dystrophin Genes, Dominant Hedgehog Proteins Limb Deformities, Congenital Kidney Diseases, Cystic Pigment Epithelium of Eye Microphthalmos Photoreceptor Cells Night Blindness Limb Buds Foot Deformities, Congenital Alstrom Syndrome Encephalocele Dark Adaptation Visual Acuity Fingers Homozygote Retinal Pigment Epithelium Extremities Mutation, Missense Hand Deformities Muscular Dystrophy, Emery-Dreifuss Fluorescein Angiography Chromosome Mapping Mice, Inbred mdx Group II Chaperonins Genetic Linkage Retinal Rod Photoreceptor Cells Usher Syndromes Optic Atrophy, Hereditary, Leber Ectromelia Macular Degeneration Retinal Cone Photoreceptor Cells Heterozygote Choroid Diseases Neuroaxonal Dystrophies Mouth Abnormalities Optic Atrophies, Hereditary Cytoplasmic Dyneins Intellectual Disability Codon, Nonsense Nerve Tissue Proteins Ciliary Motility Disorders Exons Cilia Optic Disk Drusen Dermatoglyphics Sarcoglycans Molecular Sequence Data Proteins Lod Score Lipofuscin Rats, Mutant Strains Wills Kruppel-Like Transcription Factors Visual Fields Haplotypes Base Sequence Heteroduplex Analysis Hallux Hypertelorism

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